|
|
|
 |
|
 |
| |
STIFDB - Entry Name : AT3G53480 | Stress Signals involved in |
|
STIFDB Provides Data in 2 levels:
|
|
|
Gene Description : AT3G53480
| Locus Identifier | Gene Model Name | Gene Model Description | Gene Model Type | | AT3G53480 | AT3G53480.1 | ATPDR9/PDR9 (PLEIOTROPIC DRUG RESISTANCE 9) ATPase, coupled to transmembrane movement of substances Identical to Probable pleiotropic drug resistance protein 9 (PDR9) [Arabidopsis Thaliana] (GB:Q9LFH0) similar to ATPDR5/PDR5 (PLEIOTROPIC DRUG RESISTANCE 5), ATPase, coupled to transmembrane movement of substances [Arabidopsis thaliana] (TAIR:AT2G37280.1) similar to ATPDR13/PDR13 (PLEIOTROPIC DRUG RESISTANCE 13), ATP binding / ATPase/ nucleoside-triphosphatase/ nucleotide binding [Arabidopsis thaliana] (TAIR:AT4G15215.1) similar to ABC transporter family protein [Arabidopsis thaliana] (TAIR:AT4G15236.1) similar to Pleiotropic drug resistance protein 15 (GB:Q7FMW4) similar to Pleiotropic drug resistance protein 3 (NtPDR3) (GB:Q5W274) similar to PDR-like ABC transporter [Oryza sativa (japonica cultivar-group)] (GB:CAD59575.1) contains InterPro domain ABC-2 type transporter (InterPro:IPR013525) contains InterPro domain Plant PDR ABC transporter associated (InterPro:IPR013581) contains InterPro domain AAA ATPase (InterPro:IPR003593) contains InterPro domain ABC transporter related (InterPro:IPR003439) | |
Gene Ontology Data from
TAIR
: AT3G53480
| GO Category |
GO Annotation Type |
GO ID |
GO Evidence Type |
References |
| Molecular Function | ATPase activity, coupled to transmembrane movement of substances | GO:0042626 |
ISS | Communication:1674994 |
| Cellular Compartment | plasma membrane | GO:0005886 |
IDA | Publication:501718909|PMID:16618929 |
| Biological Process | multidrug transport | GO:0006855 |
ISS | Publication:501718474|PMID:16506311 |
| |
Biological Process |
|
Molecular Function |
|
Cellular Compartment |
Click here for
Guide to GO Evidence Codes
Orthologs
| Gene Id | Sorghum bicolor | Zea mays | Glycine Max
| | AT3G53480 | -- | -- | -- |
|
|
|
 |
|
 |
|
|
|
| |
|
